Samuel Perrett, Alisia Fadini, Christopher D. M. Hutchison, Sayantan Bhattacharya, Cade Morrison, Oleksii Turkot, Mads Bregenholt Jakobsen, Michael Größler, José Licón-Saláiz, Florian Griese, Samuel Flewett, Joana Valerio, Joachim Schulz, Mykola Biednov, Yifeng Jiang, Huijong Han, Hazem Yousef, Dmitry Khakhulin, Christopher Milne, Anton Barty, Jasper J. van Thor
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引用次数: 0
摘要
X 射线自由电子激光器(XFEL)可以收集高质量的串行飞秒晶体学数据。下一代百万赫兹超导自由电子激光器有望大幅缩短数据采集时间,以更高的信噪比捕捉更多的结构,促进更复杂的实验。目前,气体动态虚拟喷嘴(GDVN)是唯一一种能够充分利用百万赫兹源重复率进行晶体学研究的传输方式。然而,在连续晶体学实验中,大量的样品消耗使其无法用于许多蛋白质靶标。在这里,我们介绍了一种按需注入液滴方法的新应用,通过为每个宏脉冲定制多液滴注入方案,该方法可在欧洲 XFEL(EuXFEL)上以 47 kHz 的频率运行。我们展示了每小时 150 000 个索引图案的收集率。我们表明,其性能和有效数据收集率与 GDVN 不相上下,而样品消耗量则减少了两个数量级。我们利用飞秒 X 射线实验终端站的大像素探测器展示了溶菌酶晶体学数据。通过校正 EuXFEL 宏脉冲序列中光子能量的系统漂移,晶体学统计数据得到了显著改善。这是 EuXFEL 以 1.38 Å 分辨率收集和报告的最高分辨率蛋白质结构。
Kilohertz droplet-on-demand serial femtosecond crystallography at the European XFEL station FXE
X-ray Free Electron Lasers (XFELs) allow the collection of high-quality serial femtosecond crystallography data. The next generation of megahertz superconducting FELs promises to drastically reduce data collection times, enabling the capture of more structures with higher signal-to-noise ratios and facilitating more complex experiments. Currently, gas dynamic virtual nozzles (GDVNs) stand as the sole delivery method capable of best utilizing the repetition rate of megahertz sources for crystallography. However, their substantial sample consumption renders their use impractical for many protein targets in serial crystallography experiments. Here, we present a novel application of a droplet-on-demand injection method, which allowed operation at 47 kHz at the European XFEL (EuXFEL) by tailoring a multi-droplet injection scheme for each macro-pulse. We demonstrate a collection rate of 150 000 indexed patterns per hour. We show that the performance and effective data collection rate are comparable to GDVN, with a sample consumption reduction of two orders of magnitude. We present lysozyme crystallographic data using the Large Pixel Detector at the femtosecond x-ray experiment endstation. Significant improvement of the crystallographic statistics was made by correcting for a systematic drift of the photon energy in the EuXFEL macro-pulse train, which was characterized from indexing the individual frames in the pulse train. This is the highest resolution protein structure collected and reported at the EuXFEL at 1.38 Å resolution.